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Cognitive ImpairmentNCT04527328

A Study to Assess the Tolerability and Efficacy of AKST1210 in Patients on Hemodialysis With Cognitive Impairment

A study testing AKST1210 and Hemodialysis in people with Cognitive Impairment and End Stage Renal Disease, run by Alkahest, Inc. at 4 sites in United States.

Completed

Finished. The study has ended and is not enrolling. Results may be posted on the official record.

Official record
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Trial summary

This study will evaluate the tolerability, feasibility, and efficacy of the AKST1210 column in subjects with end-stage renal disease with cognitive impairment (ESRD-CI) undergoing hemodialysis 3 times per week. Read more about this study

Who is it for?
Ages 40 years and older
Conditions the study is for
Cognitive Impairment, End Stage Renal Disease
What is being tested?
AKST1210 and Hemodialysis
Could I receive a placebo?
Yes, some participants may receive a placebo
How many people
10 participants
Where
4 sitesUnited States
Study dates
28 Apr 2020to 4 Jun 2021
Phase
Interventional
Are there results?
Yes, posted in the registrySummary in the doctors' view

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 40 years and older
  • All sexes
  • No healthy volunteers
  • Adult, Older adult

Who may be able to join

  • On chronic hemodialysis due to end-stage renal disease for ≥ 12 months.
  • Score on the Montreal Cognitive Assessment (MoCA) ≥ 16 and ≤ 23.
  • Body mass index (BMI) ≥ 20 and ≤ 36.
  • The subject must be able to follow the study protocol, receive the treatment in the established timeframe, and continue during the follow-up interval.
  • The subject must have sufficient visual and auditory acuity to reliably complete all study assessments.
  • Provided a signed and dated informed consent form.

Who cannot join

  • Subjects for whom adequate anticoagulation cannot be achieved. Use of antiplatelet drugs (e.g., aspirin or clopidogrel) is allowed.
  • History of hypersensitivity to heparin.
  • Pregnant or breast-feeding women or women who are planning to become pregnant.
  • Clinically significant abnormalities on Screening ECG including QT interval corrected for heart rate (QTc) (using Fridericia's correction formula) of ≥ 500 ms in men and ≥ 520 ms in women.
  • Clinically significant and unexpected abnormalities in this patient population in complete blood count, complete metabolic panel, coagulation, and thyroid stimulating hormone (TSH).
  • Subjects with a hemoglobin level < 9.0 g/dL.
Show all 9Show fewer
  • Concurrent or recent participation in another investigational clinical trial. Prior clinical trial subjects must have discontinued investigational agents at least 30 days prior to Screening.
  • Subjects planning to receive renal transplantation during the study.
  • Any other condition and/or situation that the investigator believes may interfere with the safety of the subject, study conduct, or interpretation of study data.

Trial locations and contacts

4 sites in 1 country.

United States4 sites
  • Renal Consultants Medical Group

    Granada Hills, California, 91344

  • Valley Renal Medical Group

    Northridge, California, 91324

  • Orlando Clinical Research Center

    Orlando, Florida, 32809

  • US Renal Care Kidney Research

    San Antonio, Texas, 78251

Other trials in United States

About this study

Official title: A Randomized, Double-Blind, Phase 2a Study to Evaluate the Tolerability, Feasibility, and Efficacy of AKST1210 in Patients on Hemodialysis With Cognitive Impairment Associated With End-Stage Renal Disease

This study will evaluate the tolerability, feasibility, and efficacy of the AKST1210 column in subjects with end-stage renal disease with cognitive impairment (ESRD-CI) undergoing hemodialysis 3 times per week.

Read the detailed description

In this study, approximately 26 men and women on dialysis due to end stage renal disease and who have cognitive impairment will be randomly assigned to receive AKST1210 or control during each hemodialysis session for 3 months. The primary objective is to assess the safety and tolerability of AKST1210, and secondary objectives include changes in cognitive assessments as well as the feasibility of using AKST1210 in this setting.

Being tested
AKST1210, Sham Control (No Intervention), Hemodialysis
Keywords
Renal disease, Renal failure, chronic, End stage kidney disease, Chronic kidney failure, Kidney disease, Cognitive decline, Mental deterioration, Cognition disorder
Medical subject headings
Cognitive Dysfunction, Kidney Failure, Chronic, Kidney Diseases, Cognition Disorders

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • AKST1210Device

    AKST1210

  • Sham Control (No Intervention)Other

    A covered surrogate object of similar size and shape as the investigational device

  • HemodialysisProcedure or surgery

    Hemodialysis

Study groups in NCT04527328
Study groupRoleWhat they receive
AKST1210ExperimentalThe AKST1210 column will be connected to the dialysis circuit during each dialysis session.
Receives: Device: AKST1210; Procedure: Hemodialysis
Sham Control (No Intervention)Sham comparatorA covered surrogate object of similar size and shape as the investigational device
Receives: Other: Sham Control (No Intervention); Procedure: Hemodialysis

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Number of Participants With Treatment-Emergent Adverse Events Assessed by Intensity

    Number of participants with Treatment-Emergent Adverse Events (TEAE) assessed by Intensity (mild, moderate, or severe) coded by the Medical Dictionary for Regulatory Activities (MedDRA)

    Measured: Baseline to Week 14

Secondary outcomes (14)
  1. Tolerability as Measured by the Number of Subjects Who Complete Each Treatment Period

    The number of subjects will be summarized by AKST1210 column size (small, S-15; medium, S-25; and large, S-35) and control for subjects who completed all visits in the treatment period

    Measured: Baseline to Week 12

  2. Number of Participants Who Discontinued Due to Intradialytic Hypotension (IDH)

    The number and percentage of subjects requiring early discontinuation from study treatment due to IDH summarized by treatment group

    Measured: Baseline to Week 12

  3. Change From Baseline in Montreal Cognitive Assessment (MoCA)

    Change from baseline to EOS in the total Montreal Cognitive Assessment (MoCA) score, which assesses executive functions, naming, attention and concentration, language, abstraction, delayed recall, and orientation. The MoCA has a total score from 0 to 30 whereby all sub sections are summed. The scoring breakdown for all sub sections includes the following: Visuospatial and executive functioning: 0-5 points, naming: 0-3 points, attention: 0-6 points, language: 0-3 points, abstraction: 0-2 points, delayed recall: 0- 5 points, orientation: 0-6 points. 1 point is added to the test-taker's score if they have 12 years or less of formal education. Higher scores in all sub categories and total score indicate better cognition. The Mean change from baseline is the post-treatment value minus baseline value.

    Measured: Screening to Week 14

  4. Change From Baseline in Computer-based Cognitive Assessment (CogState) Composite Score

    Mean change from baseline to End of Treatment in CogState test battery composite scores. The CogState test battery is a simple, brief computerized battery designed to assess cognitive function in several areas including verbal learning, psychomotor function, visual attention, working memory, executive function, and verbal delayed recall. Higher scores indicate better outcomes for all composite scores. All composite scores have a range of -16 to 10. Z-Scores between ≥ 1 and < 1.5 standard deviations (SD) below age-matched normative data are considered minor cognitive impairment. Z-Scores between ≥ 1.5 and < 2 SD below age-matched normative data are considered mild cognitive impairment. Z-Scores ≥ 2 SD below age matched normative data are considered major cognitive impairment consistent with dementia.

    Measured: Baseline to Week 12

  5. Change From Baseline in Quality of Life Per the Short-Form Health Survey (SF-36)

    Mean change from baseline in quality of life per the Short-Form Health Survey (SF-36), which evaluates quality of life measures. All scores range from 0 to 100 with higher scores indicating less disability. An increase or decrease in the mental health summary score or physical health summary score from baseline indicates a more favorable health status or a more unfavorable health status, respectfully, in the subject's quality of life related to mental or physical health.

    Measured: Baseline to Week 12

  6. Change From Baseline in the Patient Health Questionnaire-9 (PHQ-9)

    Change from baseline to EOS in the Patient Health Questionnaire-9 (PHQ-9), which evaluates the severity of depression. Symptoms are rated from 0 (not at all) to 3 (nearly every day) and scores are summated for each subject across the 9 items. The total score range is 0-27. An increase or decrease in the PHQ-9 total score from baseline indicates greater severity or less severity, respectfully, in the subject's state of depression.

    Measured: Baseline to Week 14

  7. Change From Baseline in Sleep Quality Per the Pittsburgh Sleep Quality Index (PSQI)

    Change from baseline in sleep quality as measured by the Sleep Quality Per the Pittsburgh Sleep Quality Index (PSQI), which measures the quality and patterns of sleep in older adults. It differentiates "poor" from "good" sleep by measuring 7 domains: subjective sleep quality, sleep latency, sleep duration, habitual sleep efficiency, sleep disturbances, use of sleep medication, and daytime dysfunction over the last month. The subject self-rates each of these 7 areas of sleep. The score for each domain ranges from 0 to 3, whereby higher scores for each reflect the negative (worse) extreme on the Likert Scale. The sum of all 7 domains is used to compute the total score (0 to 21). A global sum of "5" or greater indicates a "poor" sleeper. An increase or decrease in the PSQI total score from baseline indicates worsening or improvement, respectfully, in the subject's overall sleep quality.

    Measured: Baseline to Week 12

  8. Change From Baseline in Fatigue Per the Fatigue Questionnaire - Functional Assessments of Chronic Illness Therapy (FACIT)

    Change from baseline to End of Treatment in fatigue as measured by the Functional Assessments of Chronic Illness Therapy (FACIT), which measures an individual's level of fatigue during their usual daily activities over the past week. The level of fatigue for each question is measured on a 4-point Likert scale (4 = not at all fatigued to 0 = very much fatigued). The total score range is 0 to 52. To get this total, each question answered is scored individually, summed, multiplied by 13, and lastly divided by the number of questions answered. The higher the total score, the better the quality of life.

    Measured: Baseline to Week 12

  9. Number of Participants Who Discontinued Due to Anemia.

    The number and percentage of subjects with any anemia leading to discontinuation from AKST1210/control will be summarized by treatment group and total.

    Measured: Baseline to Week 12

  10. Tolerability as Measured by the Percentage of Subjects Who Complete Each Treatment Period

    The percentage of subjects will be summarized by AKST1210 column size (small, S-15; medium, S-25; and large, S-35) and control for subjects who completed all visits in the treatment period

    Measured: Baseline to Week 12

  11. Tolerability as Measured by the Number of Subjects Who Complete the Run-In Period.

    The number of subjects who completed the run-in period prior to randomization and initiation of study treatment. Subjects who met all eligibility criteria assessed during screening were monitored during a two-week run-in period for ongoing assessment of eligibility, safety, and baseline assessments prior to randomization and initiation of study treatment.

    Measured: Week -2 (Day -14) to Week -1 (Day -1)

  12. Tolerability as Measured by the Percentage of Subjects Who Complete the Run-in Period

    The percentage of subjects who completed the run-in period prior to randomization and initiation of study treatment. Subjects who met all eligibility criteria assessed during screening were monitored during a two-week run-in period for ongoing assessment of eligibility, safety, and baseline assessments prior to randomization and initiation of study treatment.

    Measured: Week -2 (Day -14) to Week -1 (Day -1)

  13. Tolerability as Measured by the Number of Subjects Who Completed All Visits.

    The number of subjects will be summarized by column size (small, S-15; medium, S-25; and large, S-35) and control for subjects who completed all visits

    Measured: Baseline to Week 14

  14. Tolerability as Measured by the Percentage of Subjects Who Completed All Visits.

    The percentage of subjects will be summarized by column size (small, S-15; medium, S-25; and large, S-35) and control for subjects who completed all visits

    Measured: Baseline to Week 14

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted26 Aug 2020
  2. Study start28 Apr 2020
  3. Primary completion4 Jun 2021
  4. Study completion4 Jun 2021

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Interventional
Phase
Phase N/A
Primary purpose
Treatment
Allocation
Randomised
Intervention model
Parallel groups
Masking
Triple blind
Who is masked
Participant, Investigator, Outcomes assessor
Enrolment
10 participants (actual)
IDs, dates and publications
ClinicalTrials.gov ID
NCT04527328
Sponsor's protocol ID
AKST1210-201
Status last verified
Nov 2022
First submitted
22 May 2020
Last updated
12 Dec 2022
Data monitoring committee
Yes
FDA-regulated drug
No
FDA-regulated device
Yes

Questions about this trial

What is this clinical trial studying?

A study testing AKST1210 and Hemodialysis in people with Cognitive Impairment and End Stage Renal Disease, run by Alkahest, Inc. at 4 sites in United States.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 6 inclusion and 9 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: finished, as of the sponsor's last update on 12 Dec 2022. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 4 sites in United States. Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. Some participants in this study may receive a placebo. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

Are results available for this study?

Yes. Results are posted in the registry (first posted 12 Dec 2022). A summary is in the For doctors view, and the full results are on ClinicalTrials.gov.

How can a doctor refer a patient or contact the research team?

The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Number of Participants With Treatment-Emergent Adverse Events Assessed by Intensity (time frame: Baseline to Week 14). It is what the study was designed to measure, not a finding.

Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 12 Dec 2022; AzTrials last refreshed its copy on 7 Nov 2026.

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